Hi, (I used to have an account on shift.ms connected to my facebook but it won’t let me log in this way anymore- is anyone else having that problem??) I came on here to 1. rant and 2. get advice. I was diagnosed last year with MS after a bout of numbness from my chest down. Once this went aw…

Hi everyone, I am currently studying for a degree (In England) and have just been diagnosed with RRMS. I have received equipment from the Disabled students allowance (DSA), but I don’t know what support I am supposed to be entitled to at my university. The only information I can find online i…

One of Universal Credit (UC) policy’s most shameful parts is barely being noticed. The true measure of any society can be found in how it treats its most vulnerable members: Mahatma Gandhi The hidden cuts being forced on Britain’s most severely disabled people will increase with the full roll o…

Hi there! I am a little reluctant to posting about this but here it goes. I started to slowly go crazy and I was advised to start a blog and vent about it. I believe many have come to the point you feel your reality is different that anyone else’s. If it is so please Kindly peak into my blog,…

Hi All, A few months ago I got hospitalised for weeks after lots of symptoms including eventually not being able to get around or use my hand. I was diagnosed with RRMS and recently started Tecfedira. I am a lot better generally from these symptoms but sometimes get new symptoms like numbness in va…

hi does anyone know , can you claim attendance allowance as well as PIP ????